Regulatory Compliance Manager

Are you interested in joining an agile team of experts linking medical information to regulatory requirements and ultimately commercial interests within the Dental Implants business?
About the position
We are currently looking for a Regulatory Compliance Manager to strengthen our organization. The candidate will work in an international environment with enthusiastic people and continuously develop our business to meet new demanding requirements.
Your key accountabilities are to:
Develop strategies and plans for registration of new or changed products in close cooperation with the registration holders in the target countries.
Represent the department in Product Development Projects (including medical device software), line extensions and any changes/upgrades of products in the product portfolio to guide and support the organization with regulatory advice for market access.
Compile registration documentation and manage registration of new / changed products according to the company strategies and plans.
Review device labeling, labels and advertising material for compliance with regulatory requirements and applicable laws.
Perform classification of products.
Maintain current knowledge of FDA and international regulation, guidance and standards applicable to company products.

Who you are
For this role in a truly global business environment, we look for qualified candidates with analytical skills and open for generate creative solutions in a regulated Medical Device Industry.
We believe you have:
A MSc in engineering or natural science or an equivalent professional background.
Experience from writing regulatory applications for medical devices products for entering the USA and Canada markets.
Experience from working in a medical device industry and have knowledge about ISO 13485 and 21 CFR
Experience from Medical Device Directive 93/42/EEC and insight into Medical Device Regulation (MDR 2017/745).
Strong communication skills in English, both written and spoken.

It would be an advantages if you have experience from submission of medical device software.
Good to know
Preferably we want to fill this position as soon as possible, but we prefer to find the right person rather than having anyone right now.
The position will be located in Mölndal, Sweden and reports to the Director of Regulatory Compliance. For more information, please contact recruiting manager, Lena Lindblad, telephone +46 72 52 55 751
Please note that we will review applications continuously, so be sure to send in your application as soon as possible.
About Dentsply Sirona
Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. As The Dental Solutions Company™, Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better, safer and faster dentistry. Dentsply Sirona’s global headquarters is located in York, Pennsylvania, and the international headquarters is based in Salzburg, Austria. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY.